rs10501570
From SNPedia
Orientation | plus |
Stabilized | plus |
Geno | Mag | Summary |
---|---|---|
(T;T) | 1 | Normal risk of developing Parkinson's Disease |
Make rs10501570(C;C) |
Make rs10501570(C;T) |
Reference | GRCh38 38.1/141 |
Chromosome | 11 |
Position | 84706803 |
Gene | DLG2 |
is a | snp |
is | mentioned by |
dbSNP | rs10501570 |
dbSNP (classic) | rs10501570 |
ClinGen | rs10501570 |
ebi | rs10501570 |
HLI | rs10501570 |
Exac | rs10501570 |
Gnomad | rs10501570 |
Varsome | rs10501570 |
LitVar | rs10501570 |
Map | rs10501570 |
PheGenI | rs10501570 |
Biobank | rs10501570 |
1000 genomes | rs10501570 |
hgdp | rs10501570 |
ensembl | rs10501570 |
geneview | rs10501570 |
scholar | rs10501570 |
rs10501570 | |
pharmgkb | rs10501570 |
gwascentral | rs10501570 |
openSNP | rs10501570 |
23andMe | rs10501570 |
SNPshot | rs10501570 |
SNPdbe | rs10501570 |
MSV3d | rs10501570 |
GWAS Ctlg | rs10501570 |
GMAF | 0.09734 |
Max Magnitude | 1 |
? | (C;C) (C;T) (T;T) | 28 |
---|---|---|
|
GWAS | |
---|---|
SNP | rs10501570 |
PubMedID | [PMID 17052657] |
Condition | Parkinson's disease |
Gene | DLG2 |
Risk Allele | |
pValue | 7.00E-006 |
OR | 5 |
95% CI | 2.00-12.50 |
[PMID 19208180] Detecting disease-associated genotype patterns.
[PMID 19429005] Phactr2 and Parkinson's disease.